Process for the direct hydrogenation of wax esters

ABSTRACT

This invention relates to a process for the direct hydrogenation of wax esters which comprises contacting and reacting a wax ester with hydrogen under liquid phase hydrogenation conditions in the presence of a catalyst comprising a copper compound, a zinc compound, and at least one rare earth compound.

FIELD OF THE INVENTION

This invention relates to a process for the direct hydrogenation of wax esters in the liquid phase utilizing a catalyst comprising a copper compound, a zinc compound, at least one rare earth compound, and optionally, a compound selected from the group consisting of aluminum, zirconium and mixtures thereof.

BACKGROUND OF THE INVENTION

The hydrogenation of carboxylic acids and carboxylic esters to alcohols is known in the art, and various methods and catalysts have been suggested for effecting the hydrogenation. A commonly practiced method involves the use of a copper-chromite-based hydrogenation catalyst. While copper chromite catalysts are successful and commercially available, the disposal of the spent copper chromite catalyst is a problem since chromium can exist in different oxidation states. Some of these oxidation states are reported to be toxic to humans.

SUMMARY OF THE INVENTION

This invention therefore provides a process for the direct hydrogenation of esters which comprises contacting and reacting a wax ester with hydrogen under liquid phase hydrogenation conditions in the presence of a catalyst comprising a copper compound, a zinc compound, at least one rare earth compound, and optionally, a compound selected from the group consisting of aluminum, zirconium and mixtures thereof. The catalyst composition is prepared by a process which comprising co-precipitating from aqueous solution compounds of copper, zinc, rare earth, and, if present, aluminum and/or zirconium, washing, drying and calcining the precipitate, and subsequently activating the calcined precipitate in a reducing atmosphere.

It has been found that high purity alcohols can be obtained utilizing a catalyst comprising a copper compound, a zinc compound, and at least one rare earth compound.

DESCRIPTION OF THE PREFERRED EMBODIMENTS

The present invention relates to a process for the direct hydrogenation of wax esters to form fatty alcohols. As used herein, the term "wax esters" refers to compounds, typically C₆ to C₄₄ compounds, which have been produced by ester exchange of natural triglycerides. Examples of triglycerides which can be used as raw materials to form wax esters include natural oils, such as coconut oil, rape seed oil, and palm oils, and animal fats, such as lard, tallow and fish oil. Examples of wax esters include decyl decanoate (capryl caprate), dodecyl dodecanoate (lauryl laurate), tetradecyl tetradecanoate (myristyl myristate), hexadecyl hexadecanoate (palmityl palmitate), octadecyl octadecanoate (stearate or isostearate), octadecenyl octadecenoate (oleate, linoleate or linolenate), lauryl myristate, myristyl palmitate, oleyl laurate, and docosyl docosanoate (erucyl erucate). As used herein, "fatty alcohol" refers to an alcohol, preferably a linear alcohol, containing from about 6 to about 22 carbon atoms, preferably from about 10 carbon atoms to about 22 carbon atoms. Typical fatty alcohols produced by the direct hydrogenation process of the present invention include 1-decanol, 1-dodecanol, 1-tetradecanol, 1-hexadecanol, 1-octadecanol, and the like, and mixtures thereof.

The catalyst compositions of the present invention comprise mixtures of a copper compound, a zinc compound, and at least one rare earth compound. The catalysts may additionally contain a compound selected from the group consisting of aluminum, zirconium and mixtures thereof.

The copper content of the catalyst can vary over a wide range for example, from about 10 percent by weight to about 80 percent by weight, calculated as the oxide, basis the total weight of the catalyst. However, for an optimal combination of initial catalyst activity and catalyst stability, a copper content in the range of from about 25 percent by weight to about 75 percent by weight, calculated as the oxide, is preferred, especially from about 30 percent by weight to about 70 percent by weight, calculated as the oxide. All ratios specified herein are metal atoms unless otherwise noted.

The zinc content of the catalyst is typically in the range of from about 10 percent by weight to about 80 percent by weight, calculated as the oxide, basis the total weight of the catalyst. Preferably, the zinc content of the catalyst is in the range of from about 15 percent by weight to about 75 percent by weight, calculated as the oxide, especially from about 20 percent by weight to about 70 percent by weight, calculated as the oxide. The ratio of zinc to copper in the catalyst is generally in the range of from about 1:5 to about 5:1, and preferably in the range of from about 1:4 to about 2:1.

The rare earth content of the catalyst is typically in the range of from about 0.1 percent by weight to about 20 percent by weight, calculated as the oxide, basis the total weight of the catalyst. Preferably, the rare earth content of the catalyst is in the range of from about 0.2 percent by weight to about 15 percent by weight, calculated as the oxide, especially from about 0.3 percent by weight to about 10 percent by weight, calculated as the oxide.

As used herein, the terms "rare earth" and "lanthanide" refer to the series of elements with atomic numbers ranging from 57 (lanthanum) through 71 (lutetium). With regard to the rare earth (lanthanide) series, mixed metals are readily available commercially. For purposes of the present invention, the rare earth is selected from the group consisting of praseodymium, neodymium, yttrium, lanthanum,samarium, thorium, cerium and mixtures thereof, with lanthanum being preferred.

In one embodiment, the catalyst may additionally comprise a compound selected from the group consisting of aluminum, zirconium, magnesium and mixtures thereof. When the catalyst contains aluminum and/or zirconium and/or magnesium, the aluminum and/or zirconium and/or magnesium content of the catalyst is typically in the range of from about 0.05 percent by weight to about 30 percent by weight, calculated as the oxide, basis the total weight of the catalyst. Preferably, the aluminum and/or zirconium and/or magnesium content of the catalyst is in the range of from about 0.4 percent by weight to about 20 percent by weight, calculated as the oxide, especially from about 0.6 percent by weight to about 10 percent by weight, calculated as the oxide.

Various procedures can be utilized to prepare the catalysts of the present invention. For example, individual solutions of the metals may be prepared and mixed together followed by the addition of an aqueous alkaline solution. Alternatively, a first aqueous solution comprising a copper or zinc salt and a second solution comprising a soluble base and at least one soluble salt of at least one second metal can be prepared, and these two solutions are then added simultaneously to a vessel containing water. In a preferred embodiment, the catalysts are prepared by co-precipitating from aqueous solution thermally decomposable compounds of copper, zinc, and a rare earth, washing the precipitate and calcining the precipitate to give the metal oxides. The catalyst precursor is subjected to a reduction treatment to give the active catalyst.

It is understood that the catalyst is usually handled and stored in the form of its precursor, which indeed is referred to in commerce as the "catalyst" although it is not the catalyst in the strict sense of the agent taking part in chemical reactions such as hydrogenation of wax esters. Reduction of the precursor to the catalyst is normally carried out by the operator of the chemical process. The precursor may be in shapes, e.g., pellets, as required by the user of the catalyst, or may be in its condition before the shaping operation, e.g., as powder or lightly compressed powder.

The initial form in which the copper, zinc, rare earth are employed is the oxide, although compounds which are readily converted to the oxide, e.g., the corresponding metal carbonates, are also suitable initially employed as these are converted to the oxide during pretreatment subsequent to the formation of the initially prepared catalyst composition. Pretreatment of the catalyst in hydrogen and operation of the catalyst in the reaction environment will cause at least partial reduction of some of the metals, such as copper, to lower oxidation states, and it is intended that catalysts with these reduced states will fall within the scope of this invention.

In the method of making the catalyst the reaction conditions for the precipitation should be carefully controlled. The temperature for the precipitation is preferably in the range of from about 20° C. to about 100° C., preferably from about 50° C. to about 85° C., and the pH during the precipitation process is maintained between about 5.5 and about 7.5, preferably between about 6.0 to about 7.0 and more preferably, between about 6.3 and about 6.7. The precipitating agent will be an alkali metal or an ammonium carbonate solution. The precipitate thus obtained is a mixture of carbonates, basic carbonates, oxides, hydrated oxides and hydroxides. The precipitate is washed, preferably several times with water, aged, reslurried and then dried and calcined, preferably in air at a temperature of from about 200° C. to about 400° C., with a temperature of about 250° C. to about 350° C. being preferred. The drying is carried out at a temperature sufficient to remove the water. This step is conveniently combined with the calcination by a suitable ramping of the temperature from room temperature slowly through the drying temperature, then up to calcination temperature. The calcined material is shaped, for example, by pelleting under pressure using alumina as a binder, or graphite as lubricant. The oxide mixture is pretreated in a hydrogen-containing atmosphere prior to use as a catalyst to bring it to its most active state. Pretreatment is accomplished by contacting the catalyst with a stream of hydrogen, or of hydrogen mixed with an inert gas or diluent at a temperature ranging from about 100° C. to about 400° C. Suitable diluent gases for the activating gas mixture comprise nitrogen, or oxides of carbon.

In a preferred embodiment, an aqueous solution of copper, zinc and lanthanum salts is employed. Preferably utilized are copper nitrate, zinc nitrate, and lanthanum nitrate. A second solution of alkali metal or preferably, ammonium carbonate is prepared. The two solutions are heated to a temperature of about 20° C. to about 85° C. and simultaneously metered into the precipitation container at rates such that the pH in the precipitation container is maintained between 5.5 and 7.5. Additional water may be used either initially in the precipitation container or added concurrently with the salt solution and precipitation solution. The resulting precipitate is thoroughly washed, dried, calcined at about 300° C. and activated in hydrogen at temperatures ranging from about 100° C. to about 400° C.

In the process of the present invention, one or more wax esters is contacted and reacted with hydrogen in the presence of the above-described catalyst in a reactor. The reactor may be a trickle bed reactor, fixed bed gas-solid reactor, packed bubble column reactor, continuously stirred tank reactor or a slurry phase reactor. The process may be carried out batchwise or in continuous fashion.

The reaction temperatures are typically in the range of from about 170° C. to about 250° C., preferably in the range of from about 190° C. to 240° C. and more preferably in the range of from about 205° C. to 230° C. With respect to the reaction temperatures, it is important to ensure that the temperature does not exceed 250° C. At temperatures greater than 250° C., the paraffin make increases to unacceptable levels. The reaction pressures are typically in the range of from about 300 psig to about 2000 psig, preferably in the range of from about 400 psig to about 1500 psig, and more preferably in the range of from about 500 psig to about 1000 psig. Operation at these low reaction pressures is possible due to the high activity and selectivity of the catalysts. The molar ratio of hydrogen to wax ester in the process of the present invention is in the range of from about 20:1 to about 700:1, preferably from about 350:1 to about 650:1, and more preferably, from about 400:1 to about 600:1. The process is generally carried out at a weight hourly space velocity (WHSV) in the range of from about 0.1 hr⁻¹ to about 5 hr⁻¹, preferably in the range of from about 0.1 hr¹ to about 3 hr⁻¹. The time period required for reaction will vary according to the temperature utilized, the molar ratio of hydrogen to wax ester, and the partial pressure of hydrogen. The products produced by the present process include fatty alcohols, traces of paraffins and unreacted wax esters. The products are typically separated by conventional means such as, for example, distillation, extraction, filtration, crystallization, and the like. The desired fatty alcohol products are then utilized in various applications, such as, for example detergents and personal care products.

An advantage of the present process is the conversion, i.e., greater than at least about 80 mole percent, and approaching 100%, basis wax ester, as well as the selectivity to alcohols, i.e., greater than about 97 mole percent, and approaching 100%. The process also has advantages in that it produces very pure alcohols with very low levels of paraffins.

The ranges and limitations provided in the present specification and claims are those which are believed to particularly point out and distinctly claim the present invention. It is, however, understood that other ranges and limitations which perform substantially the same function in substantially the same manner to obtain the same or substantially the same result are intended to be within the scope of the present invention as defined by the specification and claims.

The invention is further described with reference to the following examples, which are intended to illustrate certain aspects of the invention, without limiting its broader scope.

Illustrative Embodiments Example 1 Catalyst Preparation

A solution of mixed nitrates, 96 grams (0.41 mole) of cupric nitrate, 60 grams (0.2 mole) zinc nitrate, 3.3 grams (0.008 mole) lanthanum nitrate in one liter of water was heated to 85° C. and placed in a dish and funnel. In a second funnel was placed a hot 50° C. 1 molar solution of ammonium carbonate of sufficient quantity to provide an excess over the metal nitrates. Two solutions were added simultaneously over a period of about 20 minutes to a vessel containing 1 liter of vigorously stirred distilled water at 65° C. The rates of addition were adjusted so as to maintain the pH of the mixture at about pH equal to about 6.5. After the addition had been completed the slurry was aged at 85° C. for 20 minutes and then allowed to settle and washed 5 times by decantation and reslurrying before being filtered and dried. The mixed carbonates were then calcined at 300° C. for 4 hours. The resulting oxide material was compressed isostatically at 20,000 lbs. and then crushed and sieved. The results are presented in Table I.

Catalyst Testing

The catalytic testing was conducted in typical laboratory scale reactor. The reactor tube used was constructed of 316 stainless steel and included a thermowell. The tube had an outer diameter of 1 inch and an inner diameter of 0.6 inches. An equal volume of silicon carbide, (60-80 mesh) was mixed with 20.00 g of catalyst and centered in the reactor tube between two beds of enough 20 mesh silicon carbide to fill the reactor. The reactor tube was placed in a four-zone furnace equipped with controlling thermocouples and its fittings were tightened. A multi-point thermocouple was inserted in to the thermowell to allow precise monitoring of the temperatures inside the reactor tube.

The catalyst was reduced by initiating a 10.0 L/Hr flow of approx. 5% hydrogen in nitrogen at a unit pressure of 135 psig. The reactor was heated at a rate of 60° C./Hr to 200° C. The catalyst was held at 200° C. for 17 hours. While maintaining the same flow rate, the catalyst was next reduced with hydrogen for an additional 8 hours.

After reduction, the unit pressure was raised to the desired pressure, (e.g. 600 psig) by adjusting a backpressure regulator. The hydrogen flow was adjusted to the desired flow rate. The reactor temperature was adjusted to the desired setpoint and the catalyst bed temperatures were allowed to equilibrate before the feed was introduced at the desired feed rate. The feed was stored under nitrogen and heated to 60° C. and pumped to the reactor through heated insulated lines to insure proper flow. Typical operating conditions investigated were; temperatures of 150°-260° C.; WHSV of 0.1 to 5 per hour; molar hydrogen to feedstock ratios of between 20:1 and 1000:1; and unit pressures between 200 and 2000 psig. Samples of the feed and products were analyzed by GC, NMR, IR, Mass Spectroscopy and elemental analysis.

The results for hydrogenation of pure tetradecyl tetradecanoate (myristyl myristate) are shown in Table 1.

                  TABLE 1                                                          ______________________________________                                                     H.sub.2 : Feed   Conversion                                                                             Selectivity                               Temperature (°C.)                                                                   (molar)  WHSV    (% m)   (% m)                                     ______________________________________                                         (215.6)     250:1    0.15    83.0    98.7                                                  585:1    0.15    95.2    98.7                                      (226.7)     250:1    0.15    86.3    97.1                                                  585:1    0.15    99.3    97.0                                      ______________________________________                                    

As can be seen in Table 1, the present process results in conversions greater than 80 mole percent and selectivities greater than 95 mole percent. It can also be seen that conversion is dependent on H₂ : Feed ratio and selectivity is lower at higher temperatures. Both conversion and selectivity approach 100 mole percent at suitable conditions. 

What is claimed is:
 1. A process for the direct hydrogenation of wax esters which comprises contacting and reacting one or more wax esters with hydrogen under liquid phase hydrogenation conditions in the presence of a catalyst comprising a copper compound, a zinc compound and at least one rare earth compound.
 2. The process of claim 1 wherein said catalyst additionally comprises at least one compound selected from the group consisting of aluminum, zirconium magnesium and mixtures thereof.
 3. The process of claim 1 wherein said wax ester is selected from the group consisting of decyl decanoate (capryl caprate), dodecyl dodecanoate (lauryl laurate), tetradecyl tetradecanoate (myristyl myristate), hexadecyl hexadecanoate (palmityl palmitate), octadecyl octadecanoate, octadecenyl octadecenoate lauryl myristate, myristyl palmitate, oleyl laurate, docosyl docosanoate (erucyl erucate) and mixtures thereof.
 4. The process of claim 3 wherein said wax ester is myristyl myristate.
 5. The process of claim 1 wherein said catalyst contains from about 10 percent by weight to about 80 percent by weight, calculated as the oxide, basis the total weight of the catalyst, of copper.
 6. The process of claim 1 wherein said catalyst contains from about 10 percent by weight to about 80 percent by weight, calculated as the oxide, basis the total weight of the catalyst, of zinc.
 7. The process of claim 1 wherein said catalyst contains from about 0.1 percent by weight to about 20 percent by weight, calculated as the oxide, basis the total weight of the catalyst, of rare earth.
 8. The process of claim 7 wherein said rare earth is selected from the group consisting of selected from the group consisting of praseodymium, neodymium, yttrium, lanthanum, samarium, thorium, cerium and mixtures thereof.
 9. The process of claim 8 wherein said rare earth is lanthanum.
 10. The process of claim 2 wherein said catalyst contains aluminum.
 11. The process of claim 10 wherein said catalyst contains from about 0.05 percent by weight to about 30 percent by weight, basis the total weight of the catalyst, of aluminum.
 12. The process of claim 2 wherein said catalyst contains zirconium.
 13. The process of claim 12 wherein said catalyst contains from about 0.05 percent by weight to about 30 percent by weight, basis the total weight of the catalyst, of zirconium.
 14. The process of claim 1 wherein said process is carried out at a temperature in the range of from about 170° C. to about 250° C.
 15. The process of claim 1 wherein said process is carried out at a pressure in the range of from about 300 psig to about 2000 psig. 